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rs864309722

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs864309722(A;G)
Make rs864309722(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position169100904
GeneMECOM
is asnp
is mentioned by
dbSNPrs864309722
ebirs864309722
HLIrs864309722
Exacrs864309722
Varsomers864309722
Maprs864309722
PheGenIrs864309722
hapmaprs864309722
1000 genomesrs864309722
hgdprs864309722
ensemblrs864309722
gopubmedrs864309722
geneviewrs864309722
scholarrs864309722
googlers864309722
pharmgkbrs864309722
gwascentralrs864309722
openSNPrs864309722
23andMers864309722
23andMe allrs864309722
SNP Nexus

SNPshotrs864309722
SNPdbers864309722
MSV3drs864309722
GWAS Ctlgrs864309722
Max Magnitude0
ClinVar
Risk rs864309722(G;G)
Alt rs864309722(G;G)
Reference rs864309722(A;A)
Significance Pathogenic
Disease Radioulnar synostosis with amegakaryocytic thrombocytopenia 2
Variation info
Gene MECOM
CLNDBN Radioulnar synostosis with amegakaryocytic thrombocytopenia 2
Reversed 1
HGVS NC_000003.11:g.168818692T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000203299.1,